Annotation Detail
Information
- Associated Genes
- G6PD
- Associated Variants
-
G6PD p.Phe501Cys (p.F501C)
(
ENST00000369620.6,
ENST00000393562.10,
ENST00000393564.7,
ENST00000439227.6,
ENST00000696420.1,
ENST00000696421.1,
ENST00000696429.1,
ENST00000696430.1 )
G6PD p.Arg459Leu (p.R459L) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
G6PD p.Phe501Cys (p.F501C) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
G6PD p.Arg459Leu (p.R459L) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 ) - Associated Disease
- Anemia, nonspherocytic hemolytic, due to G6PD deficiency
- Source Database
- ClinVar
- Description
- NM_001360016.2(G6PD):c.[1376G>T;1502T>G] AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency
- ClinVar Allele ID
- 25419
- ClinVar Allele ID
- 1770702
- ClinVar RefSeq Alternation Syntax
- NM_001042351.3:c.1376G>T
- ClinVar RefSeq Alternation Syntax
- NM_001360016.2:c.1376G>T
- ClinVar RefSeq Alternation Syntax
- NM_001360016.2:c.1502T>G
- ClinVar RefSeq Alternation Syntax
- NM_001042351.3:c.1502T>G
- ClinVar RefSeq Alternation Syntax
- NM_000402.4:c.1592T>G
- ClinVar RefSeq Alternation Syntax
- NM_000402.4:c.1466G>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-08-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002305752
- ClinVar Disease
- Anemia, nonspherocytic hemolytic, due to G6PD deficiency
- Observed Origin Sample
- maternal
Drugs